Sklar Instruments: Medical Device Recall in 2025 - (Recall #: Z-0950-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Medical procedure kits labeled as: 1) ECONO STERILE STRABIS SCISS STR 4.5"STER 50, Model Number 96-2540; 2) ECONO STERILE STRABIS SCISS CVD 4.5"STER 50, Model Number 96-2541; 3) ECONO STERILE STRABIS SCISS STR 4.5"STER 25, Model Number 96-2542; 4) ECONO STERILE STRABISMUS SCISS STR4.5"CS/25, Model Number 96-2542M; eye surgery

Product Classification:

Class II

Date Initiated: December 3, 2024

Date Posted: January 22, 2025

Recall Number: Z-0950-2025

Event ID: 95946

Reason for Recall:

Reports of various packaging issues that may result in a breach of the sterile barrier.

Status: Ongoing

Product Quantity: 350 units

Code Information:

1) 96-2540, UDI/DI 50649111054967, Lot codes: FSS8, FSS10; 2) 96-2541, UDI/DI 50649111055087, Lot codes: FSS10; 3) 96-2542, UDI/DI 50649111055391, Lot codes: FSS10; 4) 96-2542M, UDI/DI 50649111440685, Lot codes: MSS10.

Distribution Pattern:

Domestic: Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated